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用同源尿液或Tamm-Horsfall蛋白攻击的兔子中肾小管间质性肾炎及对Tamm-Horsfall蛋白的免疫反应

Tubulointerstitial nephritis and immunologic responses to Tamm-Horsfall protein in rabbits challenged with homologous urine or Tamm-Horsfall protein.

作者信息

Mayrer A R, Kashgarian M, Ruddle N H, Marier R, Hodson C J, Richards F F, Andriole V T

出版信息

J Immunol. 1982 Jun;128(6):2634-42.

PMID:6176647
Abstract

Tubulointerstitial nephritis was produced in 19 of 23 New Zealand White rabbits challenged i.v. with adjuvant-free homologous urine for greater than or equal to 16 wk and 11 of 14 challenged with adjuvant-free rabbit Tamm-Horsfall protein for 2 to 24 wk. Lesions were identical in the two groups of rabbits and were characterized by focal mononuclear infiltrates and microscopic scarring localized to distal nephron segments identified as the thick ascending limb of the loop of Henle. Concomitant immunoglobulin deposition was not detected despite antecedent elevations in serum IgG antibody directed against Tamm-Horsfall protein in 17 of 19 and 10 of 11 affected rabbits, respectively. Peripheral lymphocytes from affected rabbits were found to be cytotoxic and underwent blast transformation in the presence of homologous urine or Tamm-Horsfall protein in vitro. These lymphocytes were shown to produce a soluble cytotoxic product upon exposure to Tamm-Horsfall protein. Neither tubulointerstitial nephritis nor this pattern of cellular and humoral immune response to Tamm-Horsfall protein was found in two age-matched control groups: one unchallenged, and the other challenged i.v. with urine that had been selectively depleted of Tamm-Horsfall protein by 95%. It is concluded that the tubulointerstitial nephritis produced in rabbits by injection of urine or Tamm-Horsfall protein is the result of a predominately cellular immune response directed against Tamm-Horsfall protein.

摘要

23只新西兰白兔中有19只经静脉注射无佐剂同源尿液,持续大于或等于16周,14只中有11只经静脉注射无佐剂兔Tamm-Horsfall蛋白,持续2至24周,从而诱发了肾小管间质性肾炎。两组兔子的病变相同,其特征为局灶性单核细胞浸润以及局限于远端肾单位节段(即Henle袢升支粗段)的显微镜下瘢痕形成。尽管19只中有17只、11只中有10只受影响兔子血清中针对Tamm-Horsfall蛋白的IgG抗体先前升高,但未检测到伴随的免疫球蛋白沉积。发现受影响兔子的外周淋巴细胞具有细胞毒性,并且在体外同源尿液或Tamm-Horsfall蛋白存在的情况下会发生母细胞转化。这些淋巴细胞在接触Tamm-Horsfall蛋白后会产生一种可溶性细胞毒性产物。在两个年龄匹配的对照组中均未发现肾小管间质性肾炎或这种对Tamm-Horsfall蛋白的细胞和体液免疫反应模式:一组未受挑战,另一组经静脉注射已被选择性去除95%的Tamm-Horsfall蛋白的尿液。得出的结论是,通过注射尿液或Tamm-Horsfall蛋白在兔子中诱发的肾小管间质性肾炎是针对Tamm-Horsfall蛋白的主要细胞免疫反应的结果。

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